|
971
|
|
|
Complement C4B (Chido/Rodgers blood group) |
C4B1, C4B12, C4B2, C4B3, C4B5, C4BD, C4B_2, C4F, CH, CO4, CPAMD3 |
|
|
972
|
|
|
Calpain 5 |
ADNIV, HTRA3, VRNI, nCL-3 |
|
|
973
|
|
|
Complement C5 |
C5D, C5a, C5b, CPAMD4, ECLZB |
|
|
974
|
|
|
Cancer susceptibility 8 |
CARLO1, CARLo-1, LINC00860 |
|
|
975
|
|
|
Complement C5a receptor 1 |
C5A, C5AR, C5R1, CD88 |
|
|
976
|
|
|
Coiled-coil domain containing 192 |
LINC01183 |
|
|
977
|
|
|
Complement C6 |
- |
|
|
978
|
|
|
C-C motif chemokine receptor 2 |
CC-CKR-2, CCR-2, CCR2A, CCR2B, CD192, CKR2, CKR2A, CKR2B, CMKBR2, MCP-1-R, PCLUD |
|
|
979
|
|
|
CDP-L-ribitol pyrophosphorylase A |
ISPD, LGMDR20, MDDGA7, MDDGC7, Nip, hISPD |
Absence of septum pellucidum, Acquired kyphoscoliosis, Agenesis of corpus callosum, Agyria, Alpha-dystroglycanopathy, Amyotrophy, Anterior segment dysgenesis, Aqueductal stenosis, Cardiovascular abnormalities, Cataract, Cerebellar atrophy, Cerebellar hypoplasia, Cobblestone lissencephaly, Communicating hydrocephalus, Congenital cerebral hernia, Congenital coloboma of iris, Congenital hydrocephalus, Congenital hypoplasia of penis, Congenital kyphoscoliosis, Congenital muscular dystrophy, Congenital muscular dystrophy without intellectual disability, Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Fetal cerebral ventriculomegaly, Frontal bossing, Fukuyama type congenital muscular dystrophy, Glaucoma, Hydrocephalus, Hydrocephalus ex-vacuo, Hypoplasia of corpus callosum, Hypoplasia of the optic nerve, Limb-girdle muscular dystrophy-dystroglycanopathy, Limb-girdle muscle atrophy, Limb-girdle muscular dystrophy, Macrocephaly, Macroglossia, Mental retardation, Microcephaly, Microcornea, Microphthalmos, Microtia, Motor delay, Muscle eye brain disease, Muscular dystrophy, Muscular dystrophy, congenital, Muscular dystrophy-dystroglycanopathy, Myopathy, Hypotonia, Neuronal heterotopia, Obstructive hydrocephalus, Optic atrophy, Pachygyria, Partial agenesis of corpus callosum, Persistent hyperplastic primary vitreous, Polymicrogyria, Posteriorly rotated ear, Retinal detachment, Retinal dysplasia, Retinal dystrophy, Specific learning disorder, Submucosal cleft palate, Syndromic microphthalmia, Walker-warburg congenital muscular dystrophy, Walker-warburg syndromeView all (51 more) |
|
980
|
|
|
Complement C7 |
- |
|
